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CADASIL Syndrome

Known as: Dementia, Hereditary Multi Infarct Type, Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy, CADASIL1 
A familial, cerebral arteriopathy mapped to chromosome 19q12, and characterized by the presence of granular deposits in small CEREBRAL ARTERIES… 
National Institutes of Health

Related topics

Related topics

16 relations
Autosomal dominant inheritanceCADASILMIn BloodLeukoencephalopathies

Narrower (1)

Familial vascular leukoencephalopathy

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2013
2013
Intermediate follow-up results from the multicenter engager European pivotal trial.
Review
2012
Review
2012
Clinico-radiological spectrum of bilateral temporal lobe hyperintensity: a retrospective review.
Bilateral temporal lobe hyperintensity (BTH) is a commonly encountered MRI finding in a wide spectrum of clinical conditions and… 
2011
2011
CADASIL with cord involvement associated with a novel and atypical NOTCH3 mutation
Background Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL) is a hereditary… 
Review
2006
Review
2006
Physiology and pathology of notch signalling system
Notch proteins encode a family of transmembrane receptors that are part of a signalling transduction system known as Notch… 
2006
2006
Heritability of MRI lesion volume in CADASIL: evidence for genetic modifiers.
BACKGROUND AND PURPOSE The phenotypic expressivity shows striking variability among individuals with CADASIL (cerebral autosomal… 
Highly Cited
2004
Highly Cited
2004
Detection of the founder effect in Finnish CADASIL families
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is an inherited… 
Highly Cited
2002
Highly Cited
2002
C455R notch3 mutation in a Colombian CADASIL kindred with early onset of stroke
Abstract—Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is caused by… 
Highly Cited
2000
Highly Cited
2000
Evaluation of DHPLC analysis in mutational scanning of Notch3, a gene with a high G‐C content
Notch3 mutations cause CADASIL, an increasingly recognized cause of subcortical ischemic stroke and vascular dementia in human… 
Review
2000
Review
2000
Hereditary Vascular Dementia Linked to Notch 3 Mutations: CADASIL in British Families
Abstract: The most common form of familial vascular dementia is considered to be CADASIL or cerebral autosomal dominant… 
1989
1989
Pulmonary endocrine cells in pulmonary arterial disease.
Pulmonary endocrine cells containing bombesin or calcitonin have been identified in human lungs by the peroxidase-antiperoxidase… 
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